FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

QUICKPAC II ONE STEP METHAMPHETAMINE TEST

K Number: K970724 · Decision May 13, 1997
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
224
Applicant Total
13
Review Days
75

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Basic Information

Device Name
QUICKPAC II ONE STEP METHAMPHETAMINE TEST
K Number
K970724
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3100
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Drial Consultants, Inc.
Date Received
February 27, 1997
Decision Date
May 13, 1997
Product Code
DKZ
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DKZ Enzyme Immunoassay, Amphetamine

Similar 510(k) Clearances

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Other Clearances by Drial Consultants, Inc.

K Number Device Name
K973269 QUIKSTRIP ONE STEP BENZODIAZEPINE TEST
K973326 QUIKPAC II ONE STEP BENZODIAZEPINE TEST
K973047 ONE STEP URINE DRUG OF ABUSE BARBITURATE TEST
K972059 QUIKPAC II ONE STEP COCAINE TEST
K972571 QUIKSTRIP ONE STEP OPIATES TEST
K972405 QUIKPAC II ONE STEP OPIATE TEST
K971926 QUIKSTRIP ONE STEP COCAINE TEST
K970395 QUIKSTRIP ONE STEP METHAMPHETAMINE
K971218 QUIKSTRIP ONE STEP AMPHETAMINE TEST
K971109 QUIKPAC II ONE STEP AMPHETAMINE TEST
Search all 13 clearances from Drial Consultants, Inc. →